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A systematic review of metabolite profiling in gestational diabetes mellitus

期刊

DIABETOLOGIA
卷 57, 期 12, 页码 2453-2464

出版社

SPRINGER
DOI: 10.1007/s00125-014-3371-0

关键词

Amino acids; Gestational diabetes mellitus; Metabolite profiling; Metabolites; Metabolomics; Systematic review

资金

  1. National Institutes of Health [R03DK096152]
  2. Robert Wood Johnson Foundation Harold Amos Medical Faculty Development Program
  3. Massachusetts General Hospital Executive Committee on Research/Multicultural Affairs Office Physician-Scientist Development Award

向作者/读者索取更多资源

Gestational diabetes mellitus is associated with adverse maternal and fetal outcomes during, as well as subsequent to, pregnancy, including increased risk of type 2 diabetes and cardiovascular disease. Because of the importance of early risk stratification in preventing these complications, improved first-trimester biomarker determination for diagnosing gestational diabetes would enhance our ability to optimise both maternal and fetal health. Metabolomic profiling, the systematic study of small molecule products of biochemical pathways, has shown promise in the identification of key metabolites associated with the pathogenesis of several metabolic diseases, including gestational diabetes. This article provides a systematic review of the current state of research on biomarkers and gestational diabetes and discusses the clinical relevance of metabolomics in the prediction, diagnosis and management of gestational diabetes. We conducted a systematic search of MEDLINE (PubMed) up to the end of February 2014 using the key term combinations of 'metabolomics,' 'metabonomics,' 'nuclear magnetic spectroscopy,' 'mass spectrometry,' 'metabolic profiling' and 'amino acid profile' combined (AND) with 'gestational diabetes'. Additional articles were identified through searching the reference lists from included studies. Quality assessment of included articles was conducted through the use of QUADOMICS. This systematic review included 17 articles. The biomarkers most consistently associated with gestational diabetes were asymmetric dimethylarginine and NEFAs. After QUADOMICS analysis, 13 of the 17 included studies were classified as 'high quality'. Existing metabolomic studies of gestational diabetes present inconsistent findings regarding metabolite profile characteristics. Further studies are needed in larger, more racially/ethnically diverse populations.

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